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Acetyl chloride → 4-Chloro-2-methyl-1-oxo-1lambda~5~-pyridine

HRID 357575
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 357575
[CH3:1][C:2]1[CH:7]=[C:6]([N+]([O-])=O)[CH:5]=[CH:4][N+:3]=1[O-:11].C([Cl:15])(=O)C.C(=O)([O-])[O-].[Na+].[Na+]>>[Cl:15][C:6]1[CH:5]=[CH:4][N+:3]([O-:11])=[C:2]([CH3:1])[CH:7]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 6367Acetyl chlorideHCID 10340Sodium CarbonateHCID 95291Pyridine, 2-methyl-4-nitro-, 1-oxide

Produkt 1

HCID 122118014-Chloro-2-methyl-1-oxo-1lambda~5~-pyridineAusbeute 32,7 %

Versuchsvorschrift

15.4 g (0.1 mol) of 2-methyl-4-nitropyridine 1-oxide was added to 78.5 g (1 mol) of acetyl chloride at -10° C. The obtained mixture was stirred under cooling with ice for 0.5 hour. After the completion of the reaction, 300 ml of ice-water was added to the reaction mixture. The obtained mixture was neutralized with sodium carbonate and extracted with chloroform. The extract was dried over magnesium sulfate and filtered. The filtrate was concentrated under a reduced pressure and purified by silica gel column chromatography (ethyl acetate/n-hexane/methanol) to obtain 4.7 g of the title compound.

Aufarbeitung

  1. temperatureunder cooling with ice for 0.5 hour
  2. additionwas added to the reaction mixture
  3. extractionextracted with chloroform
  4. dry with materialThe extract was dried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationThe filtrate was concentrated under a reduced pressure
  7. custompurified by silica gel column chromatography (ethyl acetate/n-hexane/methanol)

Quellen und Nachweise

ORD-Eintrag
ord-743aec568dbb4f9fb0d7ff56d8c684aa
Quelldatensatz
uspto-grants-1998_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05840910

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